Registry for Study of Coils in Intracranial Aneurysms

NCT01000675 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 114

Last updated 2019-06-06

No results posted yet for this study

Summary

The current proposal describes a post-market, clinical registry of HydroSoft, aimed at gaining robust clinical data in a large set of patients to better define the advantages, and potentially, the disadvantages of the HydroSoft, and to inform future randomized trials.

Conditions

  • Cerebral Aneurysms

Sponsors & Collaborators

  • Abbott

    collaborator INDUSTRY
  • Albany Medical College

    collaborator OTHER
  • Asan Medical Center

    collaborator OTHER
  • Baylor University

    collaborator OTHER
  • Bronson Methodist Hospital

    collaborator UNKNOWN
  • Capital Health, Canada

    collaborator OTHER
  • The Cleveland Clinic

    collaborator OTHER
  • Dalhousie University

    collaborator OTHER
  • Fudan University

    collaborator OTHER
  • Fort Sanders Regional Medical Center

    collaborator UNKNOWN
  • JFK Medical Center, Florida

    collaborator OTHER
  • Kobe City Medical Center

    collaborator UNKNOWN
  • Methodist Research Institute, Indianapolis

    collaborator OTHER
  • Medical University of South Carolina

    collaborator OTHER
  • Providence Health & Services

    collaborator OTHER
  • Scott and White Hospital & Clinic

    collaborator OTHER
  • Stony Brook University

    collaborator OTHER
  • Thomas Jefferson University

    collaborator OTHER
  • Royal University Hospital Foundation

    collaborator OTHER
  • University of California, Los Angeles

    collaborator OTHER
  • University of Florida

    collaborator OTHER
  • University of Maryland

    collaborator OTHER
  • University of Oklahoma

    collaborator OTHER
  • University of Southern California

    collaborator OTHER
  • Washington University School of Medicine

    collaborator OTHER
  • Mayo Clinic

    lead OTHER

Principal Investigators

  • David F Kallmes, MD · Mayo Clinic

Eligibility

Min Age
21 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-08-31
Primary Completion
2013-06-30
Completion
2016-12-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01000675 on ClinicalTrials.gov